Evidence map›Paper›PMID 29888284›Full record

ArticleBioMed research international2018

Observations of the Effects of Angiotensin II Receptor Blocker on Angiotensin II-Induced Morphological and Mechanical Changes in Renal Tubular Epithelial Cells Using Atomic Force Microscopy.

Jin Sug Kim, Gi-Ja Lee, Tae Won Lee, Chun Gyoo Ihm, Yu Ho Lee, Yang Gyun Kim, Ju-Young Moon, Sang Ho Lee, Ji-Hye Kim, Sung-Wook Kang and 3 more

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 55% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Jin Sug KimDivision of Nephrology, Department of Internal Medicine, Kyung Hee University School of Medicine, Seoul, Republic of Korea.ORCID 0000-0001-7361-8715
Gi-Ja LeeDepartment of Biomedical Engineering, Kyung Hee University School of Medicine, Seoul, Republic of Korea.
Tae Won LeeDivision of Nephrology, Department of Internal Medicine, Kyung Hee University School of Medicine, Seoul, Republic of Korea.
Chun Gyoo IhmDivision of Nephrology, Department of Internal Medicine, Kyung Hee University School of Medicine, Seoul, Republic of Korea.
Yu Ho LeeDivision of Nephrology, Department of Internal Medicine, Kyung Hee University School of Medicine, Seoul, Republic of Korea.
Yang Gyun KimDivision of Nephrology, Department of Internal Medicine, Kyung Hee University School of Medicine, Seoul, Republic of Korea.
Ju-Young MoonDivision of Nephrology, Department of Internal Medicine, Kyung Hee University School of Medicine, Seoul, Republic of Korea.
Sang Ho LeeDivision of Nephrology, Department of Internal Medicine, Kyung Hee University School of Medicine, Seoul, Republic of Korea.ORCID 0000-0001-9915-6221
Ji-Hye KimDepartment of Biomedical Engineering, Kyung Hee University School of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-2366-9984
Sung-Wook KangDepartment of Biomedical Engineering, Kyung Hee University School of Medicine, Seoul, Republic of Korea.
Su-Jin ChaeDepartment of Biomedical Engineering, Kyung Hee University School of Medicine, Seoul, Republic of Korea.
Hun-Kuk ParkDepartment of Biomedical Engineering, Kyung Hee University School of Medicine, Seoul, Republic of Korea.
Kyung Hwan JeongDivision of Nephrology, Department of Internal Medicine, Kyung Hee University School of Medicine, Seoul, Republic of Korea.ORCID 0000-0003-1492-8021
Kyung Hee University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAngiotensin II (Ang II) plays a profibrotic role in the kidneys. Although many pathways of Ang II have been discovered, the morphological and mechanical aspects have not been well investigated. We observed the changes in tubular epithelial cells (TECs) after Ang II treatment with or without Ang II receptor blockers (ARBs) using atomic force microscopy (AFM).

methodsTECs were stimulated with Ang II with or without telmisartan, PD123319, and blebbistatin. AFM was performed to measure the cellular stiffness, cell volume, and cell surface roughness. Epithelial to mesenchymal transition markers were determined via immunocytochemistry.

resultsAfter Ang II stimulation, cells transformed to a flattened and elongated mesenchymal morphology. Cell surface roughness and volume significantly increased in Ang II treated TECs. Ang II also induced an increase in phospho-myosin light chain and F-actin and a decrease in E-cadherin. Ang II coincubation with either telmisartan or blebbistatin attenuated these Ang II-induced changes.

conclusionWe report, for the first time, the use of AFM in directly observing the changes in TECs after Ang II treatment with or without ARBs. Simultaneously, we successfully measured the selective effect of PD123319 or blebbistatin. AFM could be a noninvasive evaluating strategy for cellular processes in TECs.

Indexed as

Angiotensin IIAngiotensin Receptor AntagonistsAnimalsBenzimidazolesBenzoatesCadherinsEpithelial CellsEpithelial-Mesenchymal TransitionImidazolesKidney Tubules, DistalMicroscopy, Atomic ForcePyridinesRatsTelmisartanAngiotensin IIAngiotensin Receptor AntagonistsBenzimidazolesBenzoatesCadherinsImidazolesPD 123319PyridinesTelmisartan

Identifiers

PMID29888284
PMCPMC5985133
OpenAlexW2804793651

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.